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NCT06661473 · ClinicalTrials.gov registry record · NA

Interventional Study Exploring the Occurrence of Surgical Site Infections.

A NA study of Total Knee Arthroplasty and Total Hip Arthroplasty Revision, sponsored by Molnlycke Health Care AB.

Active
Registry status
NA
Development phase
105
Enrollment target
8
Study locations

NCT06661473 is a NA study of Total Knee Arthroplasty and Total Hip Arthroplasty Revision that is active but no longer recruiting, run by Molnlycke Health Care AB. The registered enrollment target is 105 participants, below the 291-participant average among 29 other Total Knee Arthroplasty trials with a reported enrollment target (64% lower). The trial reports 8 study locations across 8 states.

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The verdict

NCT06661473, a NA study of Total Knee Arthroplasty and Total Hip Arthroplasty Revision, is active but no longer recruiting, sponsored by Molnlycke Health Care AB.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
105 participants
Enrollment target
8
Study locations

Study Summary

Interventional study exploring surgical site complication occurrences in high-risk revision patients undergoing TKA or THA using NPWT.

Interventions

  • DEVICE Avance Solo Negative Pressure Wound Therapy

Study Locations (8)

District of Columbia

  • MedStar Health - Washington D.C.

Indiana

  • Ortho Indy - Indianapolis

Maryland

  • Life Bridge Health- Sinai Hospital - Baltimore

Minnesota

  • Twin Cities Orthopedics - Minneapolis

Missouri

  • St. Louis University - St Louis

New York

  • Northwell - Garden City

Ohio

  • Bon Secours Mercy Health - Youngstown

Washington

  • Spokane Joint Replacement Center - Spokane

Trial Details

FieldValue
Enrollment Target 105 participants
Start Date 2024-10-03
Est. Completion 2026-01
Phase NA

Sponsor

Molnlycke Health Care AB

20 total trials

What the Registry Record Tells You About NCT06661473

The ClinicalTrials.gov registry entry for NCT06661473 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 105 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 291-participant average among 29 other Total Knee Arthroplasty trials with a reported enrollment target (64% lower). The listed sponsor is Molnlycke Health Care AB, which has 20 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Total Knee Arthroplasty appearing as the primary indexed condition, and to 1 intervention - of which Avance Solo Negative Pressure Wound Therapy is the first listed.

NCT06661473 reports 8 study locations spanning 8 distinct geographic areas - top geographies include District of Columbia, Indiana, Maryland.

Frequently Asked Questions

What is clinical trial NCT06661473 about?

NCT06661473 is a clinical study titled "Interventional Study Exploring the Occurrence of Surgical Site Infections.". Interventional study exploring surgical site complication occurrences in high-risk revision patients undergoing TKA or THA using NPWT.

What is the current status of trial NCT06661473?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 105 participants. The study started on 2024-10-03. Estimated completion is 2026-01.

What conditions does trial NCT06661473 study?

This clinical trial studies the following conditions: Total Knee Arthroplasty, Total Hip Arthroplasty Revision, Total Knee Arthroplasty Revision.

What interventions are being tested in trial NCT06661473?

The interventions under investigation include: Avance Solo Negative Pressure Wound Therapy (DEVICE).

Who is sponsoring clinical trial NCT06661473?

This trial is sponsored by Molnlycke Health Care AB, which has 20 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06661473 being conducted?

This trial has 8 study locations across District of Columbia, Indiana, Maryland, Minnesota, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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